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Matrix‐assisted laser desorption/ionisation time‐of‐flight characterisation of biodegradable aliphatic copolyesters
Author(s) -
Carroccio Sabrina,
Rizzarelli Paola,
Puglisi Concetto
Publication year - 2000
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/1097-0231(20000830)14:16<1513::aid-rcm57>3.0.co;2-c
Subject(s) - chemistry , molar mass , condensation polymer , copolymer , desorption , adipate , matrix assisted laser desorption/ionization , mass spectrometry , size exclusion chromatography , polymer chemistry , mass spectrum , polystyrene , analytical chemistry (journal) , polymer , organic chemistry , chromatography , adsorption , enzyme
Matrix‐assisted laser desorption/ionisation time‐of‐flight (MALDI‐TOF) and the off‐line size exclusion chromatography matrix‐assisted laser desorption/ionisation (SEC/MALDI) method has been applied to the structural characterisation and the molar mass (MM) determination of a series of biodegradable copolyesters synthesised by high temperature melt polycondensation reaction, and of two commercial copolyesters with the trade name Bionolle. The MALDI‐TOF spectra of these copolymers showed the presence of cyclic oligomers in the lower mass region, in accord with expectations from polycondensation kinetics, and the presence of all linear species expected from their method of synthesis. The presence of unexpected linear species with olefin and carboxyl as end groups suggested the occurrence of undesirable thermal degradation processes during the melt polycondensation reaction. The absolute average molar masses obtained by the SEC‐MALDI method turned out to be lower, by a factor of about two for succinate/adipate copolymers, and by a factor of three for succinate/sebacate copolymers, with respect to those computed by using polystyrene standards in SEC. Furthermore, the MALDI‐TOF spectra of SEC fractions allowed not only the detection of linear and cyclic oligomers contained in these samples, but also the simultaneous determination of the average molar mass of both cyclic and linear oligomers. Due to the smaller hydrodynamic volume of cyclic chains with respect to linear ones, the ratio ( M cycle / M linear ) Ve at a fixed elution volume was found to be 1.25, in good agreement with the theoretical value of 1.24. Copyright © 2000 John Wiley & Sons, Ltd.